Canonical Allele Identifier: CA2428552576

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255300_49255304delinsTTGGA , CM000685.2:g.49255300_49255304delinsTTGGA	GRCh38
NC_000023.10:g.49111761_49111765delinsTTGGA , CM000685.1:g.49111761_49111765delinsTTGGA	GRCh37
NC_000023.9:g.48998705_48998709delinsTTGGA	NCBI36
NG_007392.1:g.14524_14528delinsTCCAA , LRG_62:g.14524_14528delinsTCCAA
NG_021311.2:g.24836_24840delinsTTGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.711+125_711+129delinsTCCAA	ENSP00000365372.2:n.711+125_711+129delinsTCCAA
ENST00000376207.10:c.816+125_816+129delinsTCCAA MANE Select	ENSP00000365380.4:n.816+125_816+129delinsTCCAA
ENST00000455775.7:c.885+125_885+129delinsTCCAA	ENSP00000396415.3:n.885+125_885+129delinsTCCAA
ENST00000518685.6:c.735+411_735+415delinsTCCAA	ENSP00000428952.2:n.735+411_735+415delinsTCCAA
ENST00000557224.6:c.711+125_711+129delinsTCCAA	ENSP00000451208.1:n.711+125_711+129delinsTCCAA
ENST00000651307.1:c.816+125_816+129delinsTCCAA	ENSP00000498454.1:n.816+125_816+129delinsTCCAA
ENST00000376197.1:c.666+125_666+129delinsTCCAA	ENSP00000365369.1:n.666+125_666+129delinsTCCAA
ENST00000376199.6:c.711+125_711+129delinsTCCAA	ENSP00000365372.2:n.711+125_711+129delinsTCCAA
ENST00000376207.8:c.816+125_816+129delinsTCCAA	ENSP00000365380.4:n.816+125_816+129delinsTCCAA
ENST00000455775.6:c.885+125_885+129delinsTCCAA	ENSP00000396415.3:n.885+125_885+129delinsTCCAA
ENST00000518685.5:c.711+125_711+129delinsTCCAA	ENSP00000428952.1:n.711+125_711+129delinsTCCAA
ENST00000557224.5:c.711+125_711+129delinsTCCAA	ENSP00000451208.1:n.711+125_711+129delinsTCCAA
NM_001114377.1:c.711+125_711+129delinsTCCAA	NP_001107849.1:n.711+125_711+129delinsTCCAA
NM_014009.3:c.816+125_816+129delinsTCCAA , LRG_62t1:c.816+125_816+129delinsTCCAA	NP_054728.2:n.816+125_816+129delinsTCCAA
XM_006724533.2:c.885+125_885+129delinsTCCAA	XP_006724596.2:n.885+125_885+129delinsTCCAA
XM_011543915.1:c.1035+125_1035+129delinsTCCAA	XP_011542217.1:n.1035+125_1035+129delinsTCCAA
XM_011543916.1:c.1035+125_1035+129delinsTCCAA	XP_011542218.1:n.1035+125_1035+129delinsTCCAA
XM_011543917.1:c.834+125_834+129delinsTCCAA	XP_011542219.1:n.834+125_834+129delinsTCCAA
XM_011543918.1:c.1071+125_1071+129delinsTCCAA	XP_011542220.1:n.1071+125_1071+129delinsTCCAA
XM_011543919.1:c.1035+125_1035+129delinsTCCAA	XP_011542221.1:n.1035+125_1035+129delinsTCCAA
XM_017029567.1:c.762+125_762+129delinsTCCAA	XP_016885056.1:n.762+125_762+129delinsTCCAA
NM_001114377.2:c.711+125_711+129delinsTCCAA	NP_001107849.1:n.711+125_711+129delinsTCCAA
NM_014009.4:c.816+125_816+129delinsTCCAA MANE Select	NP_054728.2:n.816+125_816+129delinsTCCAA